JP2017537137A - Pargの阻害剤としての2,4−ジオキソ−キナゾリン−6−スルホンアミド誘導体 - Google Patents

Pargの阻害剤としての2,4−ジオキソ−キナゾリン−6−スルホンアミド誘導体 Download PDF

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JP2017537137A
JP2017537137A JP2017531303A JP2017531303A JP2017537137A JP 2017537137 A JP2017537137 A JP 2017537137A JP 2017531303 A JP2017531303 A JP 2017531303A JP 2017531303 A JP2017531303 A JP 2017531303A JP 2017537137 A JP2017537137 A JP 2017537137A
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methyl
sulfonamide
dioxo
quinazoline
methylcyclopropyl
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Japanese (ja)
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イー.マクゴナグル アリソン
イー.マクゴナグル アリソン
ジョーダン アラン
ジョーダン アラン
バシュコビチ ボフダン
バシュコビチ ボフダン
ハットン コリン
ハットン コリン
ワッデル イアン
ワッデル イアン
アール.ヒッチン ジェイムズ
アール.ヒッチン ジェイムズ
メアリー スミス ケイト
メアリー スミス ケイト
エム.ハミルトン ナイル
エム.ハミルトン ナイル
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キャンサー リサーチ テクノロジー リミティド
キャンサー リサーチ テクノロジー リミティド
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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/70Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
    • C07D239/72Quinazolines; Hydrogenated quinazolines
    • C07D239/95Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in positions 2 and 4
    • C07D239/96Two oxygen atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/517Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • C07D217/00Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
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    • C07D217/24Oxygen atoms
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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D237/00Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
    • C07D237/26Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings condensed with carbocyclic rings or ring systems
    • C07D237/30Phthalazines
    • C07D237/32Phthalazines with oxygen atoms directly attached to carbon atoms of the nitrogen-containing ring
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    • C07D239/70Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
    • C07D239/72Quinazolines; Hydrogenated quinazolines
    • C07D239/86Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 4
    • C07D239/88Oxygen atoms
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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/70Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
    • C07D239/72Quinazolines; Hydrogenated quinazolines
    • C07D239/86Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 4
    • C07D239/88Oxygen atoms
    • C07D239/90Oxygen atoms with acyclic radicals attached in position 2 or 3
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
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    • C07D239/70Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
    • C07D239/72Quinazolines; Hydrogenated quinazolines
    • C07D239/86Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 4
    • C07D239/88Oxygen atoms
    • C07D239/91Oxygen atoms with aryl or aralkyl radicals attached in position 2 or 3
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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
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    • C07D241/38Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems with only hydrogen or carbon atoms directly attached to the ring nitrogen atoms
    • C07D241/40Benzopyrazines
    • C07D241/44Benzopyrazines with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the hetero ring
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    • C07D401/06Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
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    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
JP2017531303A 2014-12-12 2015-12-11 Pargの阻害剤としての2,4−ジオキソ−キナゾリン−6−スルホンアミド誘導体 Pending JP2017537137A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB1422098.2 2014-12-12
GB201422098 2014-12-12
PCT/GB2015/053883 WO2016092326A1 (fr) 2014-12-12 2015-12-11 Dérivés de 2,4-dioxo-quinazoline-6-sulfonamide en tant qu'inhibiteurs de la parg

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JP2017537137A true JP2017537137A (ja) 2017-12-14

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JP2017531303A Pending JP2017537137A (ja) 2014-12-12 2015-12-11 Pargの阻害剤としての2,4−ジオキソ−キナゾリン−6−スルホンアミド誘導体

Country Status (15)

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US (1) US10239843B2 (fr)
EP (1) EP3230273A1 (fr)
JP (1) JP2017537137A (fr)
KR (1) KR20170093967A (fr)
CN (1) CN107207467A (fr)
AU (1) AU2015359082A1 (fr)
BR (1) BR112017012402A2 (fr)
CA (1) CA2969296A1 (fr)
IL (1) IL252575A0 (fr)
MA (1) MA41140A (fr)
MX (1) MX2017007478A (fr)
RU (1) RU2017124425A (fr)
SG (1) SG11201704686UA (fr)
WO (1) WO2016092326A1 (fr)
ZA (1) ZA201704382B (fr)

Cited By (1)

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Publication number Priority date Publication date Assignee Title
WO2022138812A1 (fr) * 2020-12-24 2022-06-30 モジュラス株式会社 Composé de tétrahydrothiénopyridinesulfonamide

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WO2023057394A1 (fr) 2021-10-04 2023-04-13 Forx Therapeutics Ag Dérivés de n,n-diméthyl-4-(7-(n-(1-méthylcyclopropyl)sulfamoyl)-imidazo[1,5-a]pyridin-5-yl)pipérazine-1-carboxamide et dérivés correspondants de pyrazolo[1,5-a]pyridine utilisés en tant qu'inhibiteurs de parg pour le traitement du cancer
AU2022359801A1 (en) 2021-10-04 2024-02-01 Forx Therapeutics Ag Parg inhibitory compounds
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WO2023165571A1 (fr) * 2022-03-04 2023-09-07 上海璎黎药业有限公司 Composé contenant une structure cyclique hétéroaromatique à cinq chaînons, composition pharmaceutique et utilisation associées
WO2023175185A1 (fr) 2022-03-17 2023-09-21 Forx Therapeutics Ag Dérivés de 2,4-dioxo-1,4-dihydroquinazoline utilisés en tant qu'inhibiteurs de parg pour le traitement du cancer
WO2023175184A1 (fr) 2022-03-17 2023-09-21 Forx Therapeutics Ag Dérivés de 2,4-dioxo-1,4-dihydroquinazoline utilisés comme inhibiteurs de parg pour le traitement du cancer
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US11939335B2 (en) 2022-05-17 2024-03-26 858 Therapeutics, Inc. Substituted imidazo[1,2-a]quinazolines and imidazo [1,2-a]pyrido[4,3-e]pyrimidines as inhibitors of PARG
WO2024017306A1 (fr) * 2022-07-19 2024-01-25 苏州信诺维医药科技股份有限公司 Composé cyclique hétéroaromatique contenant du soufre, composition pharmaceutique de celui-ci et son utilisation
EP4311829A1 (fr) 2022-07-28 2024-01-31 Nodus Oncology Limited Dérivés d'hétéroaryl sulfonamide bicyclique substitués pour le traitement du cancer
WO2024074497A1 (fr) 2022-10-03 2024-04-11 Forx Therapeutics Ag Composé inhibiteur de parg

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2022138812A1 (fr) * 2020-12-24 2022-06-30 モジュラス株式会社 Composé de tétrahydrothiénopyridinesulfonamide

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CN107207467A (zh) 2017-09-26
CA2969296A1 (fr) 2016-06-16
MA41140A (fr) 2017-10-17
ZA201704382B (en) 2019-09-25
KR20170093967A (ko) 2017-08-16
IL252575A0 (en) 2017-07-31
US10239843B2 (en) 2019-03-26
BR112017012402A2 (pt) 2017-12-26
SG11201704686UA (en) 2017-07-28
RU2017124425A (ru) 2019-01-14
EP3230273A1 (fr) 2017-10-18
US20180016242A1 (en) 2018-01-18
MX2017007478A (es) 2018-05-04
AU2015359082A1 (en) 2017-06-29
WO2016092326A1 (fr) 2016-06-16

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